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1.
Mol Biol Rep ; 49(6): 5153-5163, 2022 Jun.
Article in English | MEDLINE | ID: mdl-35169998

ABSTRACT

INTRODUCTION: The coronavirus disease (COVID-19) is caused by the severe acute syndrome coronavirus-2 (SARS-COV-2) and still threatens human life. This pandemic is still causing increased mortality throughout the world. Many recent studies have been conducted to discover the pathophysiology of this virus. MATERIAL AND METHODS: However, in this narrative review, we attempted to summarize some of the alterations in physiological pathways that were evident in this viral invasion. Excessive inflammation that progresses to cytokine storm, changes in humoral and cell-mediated immunity, and observed alterations in iron metabolism are included in the pathogenesis of the virus. Iron homeostasis disturbances may persist for more than two months after the onset of COVID-19, which may lead to reduced iron bioavailability, hypoferremia, hyperferritinemia, impaired hemoglobin, and red blood cell synthesis. Furthermore, hypoferriemia may impair immune system function. Until now, the traditional treatments discovered are still being tried. RESULTS: However, using probiotics as an adjuvant was shown to have beneficial effects on both iron homeostasis and immunity in COVID-19. Herein, we discussed the possible mechanisms achieved by probiotics to ameliorate iron and immunity changes based on the available literature. CONCLUSION: We concluded that supplementing probiotics with conventional therapy may improve COVID-19 symptoms and outcomes. Taking into consideration the use of good quality probiotics and appropriate dosage, undesirable effects can be avoided.


Subject(s)
COVID-19 , Probiotics , Homeostasis , Humans , Inflammation/metabolism , Iron/metabolism , Probiotics/therapeutic use , SARS-CoV-2
2.
J Nutr Metab ; 2019: 1431384, 2019.
Article in English | MEDLINE | ID: mdl-31049223

ABSTRACT

Osteoporosis poses an important public health problem which affects millions of people worldwide. There is a direct link between calcium deficiency in diet and induction of osteoporosis and bone loss. The current study was conducted to evaluate the protective effect of thyme (Thymus vulgaris L.) and rosemary (Rosmarinus officinalis L.) against osteoporosis in rats with low calcium intake. Essential oils of rosemary and thyme were analyzed. The experiment was carried out on growing male Sprague-Dawley rats; the experimental animals were divided into 5 groups: 1, control negative was fed standard balanced diet; 2, control positive was fed balanced diet with low calcium level (L Ca) (Ca 0.1% w/w); 3, (L Ca) + thyme powder (5% w/w); 4, (L Ca) + rosemary powder (5% w/w); 5, (L Ca) + orally administration with CaCO3 (27 mg/kg body weight). Blood samples were collected for different biochemical analyses in plasma (calcium (Ca), phosphorus (P), magnesium (Mg), tumor necrosis factor-alpha (TNF-α), C-reactive protein (CRP), malondialdehyde (MDA), parathyroid hormone (PTH), C-terminal telopeptide (CTX), and 1,25-(OH)2-vitamin D3). Femur mass, length, and bone mineral density (BMD) were recorded, and histopathological studies for femurs were examined. Low-calcium diet induced osteoporotic changes in positive control rats (decrease in Ca, vitamin D3, and BMD and increase in CTX, PTH, TNF-α, CRP, and MDA). Supplementation with thyme and rosemary inhibited significantly the development of bone loss, increased Ca and vitamin D3 in plasma, improved BMD, and also prevented the inflammation and oxidative stress (improved TNF-α, CRP and MDA) compared to the positive control. The histopathological examination of treated groups showed an improvement in bone histology and protection against bone loss. However, thyme powder showed more effective impact than rosemary. Our study demonstrates that thyme and rosemary effectively mitigated calcium deficiency-induced bone loss and maybe considered as promising candidates for preventing bone resorption and osteoporosis.

3.
J Complement Integr Med ; 16(3)2019 Feb 05.
Article in English | MEDLINE | ID: mdl-30726190

ABSTRACT

Dietary antioxidants are widely distributed in various types of our food. They are strongly associated with reduced risk of many chronic diseases such as atherosclerosis, cancer, and Alzheimer's diseases. They include vitamins such as vitamins A, E, C, and carotenoids. Also, some minerals like; zinc, manganese, copper, iron, and selenium are essential for the activity of antioxidant enzymes. Furthermore, dietary polyphenols and flavonoids are considered as potent antioxidant compounds. Vegetables, fruits, and edible herbs are the richest sources of such antioxidants. Antioxidants reduce oxidative stress, either directly by reducing reactive species or indirectly by enhancing the body antioxidant defense mechanisms in different ways. These may include upregulating gene expression of some antioxidant enzymes via a nuclear factor erythroid 2 related factor2 pathway. Administration of a mixture of antioxidants is beneficial since they act synergistically in various phases. The aims of this review are to summarize the different antioxidants from dietary sources and their role in the prevention of different diseases.


Subject(s)
Antioxidants/metabolism , NF-E2-Related Factor 2/metabolism , Preventive Medicine , Animals , Dietary Supplements/analysis , Disease/genetics , Humans , NF-E2-Related Factor 2/genetics
4.
J Diet Suppl ; 15(3): 300-310, 2018 May 04.
Article in English | MEDLINE | ID: mdl-28759296

ABSTRACT

The purpose of this study was to illustrate the effects of zinc oxide nanoparticles (ZnO-NPs) administration on bone turnover and bone resorbing agents in rats and how L-arginine (L-arg) or vitamin E (vit E) co-administrations might affect them. Fasting rats were randomly divided into four groups (n = 10): G1-normal healthy animals; G2-ZnO-NPs-exposed rats (600 mg/kg-1/day-1); G3-ZnO-NPs-exposed rats co-administrated L-arg (200 mg/kg-1/day-1); G4-ZnO-NPs-exposed rats co-administrated vit E (200 mg/kg-1/day-1). The ingredients were orally administered daily. The body weight and food consumption of rats were recorded during the administration period and the experiment continued for three consecutive weeks. The results demonstrated that ZnO-NPs administration induced bone loss in rats as manifested by reduced activity of bone alkaline phosphatase (B-ALP) and increased level of C-terminal peptide type I collagen (CTx). The increase of inflammatory markers, tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) by ZnO-NPs suggests that deleterious effects of ZnO-NPs on bone turnover were, in part, due to inflammation. Confirming to this suggestion, both L-arg and vit E reduced TNF-α and IL-6 levels and consequently decreased bone resorption as indicated by reduced serum CTx level. This study proved that ZnO-NPs can induce bone turnover, which may be reduced by L-arg or vit.E co-administration, partly by anti-inflammatory mechanism.


Subject(s)
Arginine/therapeutic use , Dietary Supplements , Metal Nanoparticles/toxicity , Osteoporosis/prevention & control , Protective Agents/therapeutic use , Vitamin E/therapeutic use , Zinc Oxide/toxicity , Administration, Oral , Animals , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antioxidants/therapeutic use , Biomarkers/blood , Bone Density Conservation Agents/therapeutic use , Bone Remodeling/drug effects , Bone and Bones/drug effects , Bone and Bones/immunology , Environmental Pollutants/administration & dosage , Environmental Pollutants/antagonists & inhibitors , Environmental Pollutants/toxicity , Inflammation Mediators/blood , Metal Nanoparticles/administration & dosage , Metal Nanoparticles/chemistry , Osteitis/blood , Osteitis/chemically induced , Osteitis/immunology , Osteitis/prevention & control , Osteoporosis/blood , Osteoporosis/chemically induced , Osteoporosis/immunology , Random Allocation , Rats, Wistar , Zinc Oxide/administration & dosage , Zinc Oxide/antagonists & inhibitors
5.
J Diet Suppl ; 14(4): 380-394, 2017 Jul 04.
Article in English | MEDLINE | ID: mdl-27973970

ABSTRACT

Gentamicin (GM) is a drug used commonly against gram-negative bacteria. Its therapeutic use is mainly limited by its nephrotoxicity. This investigation was aimed at evaluating the nephroprotective effects of rosemary (RM; Rosmarinus officinalis) and thyme (TV; Thymus vulgaris) against GM toxicity. Rats were divided into four groups. Normal control group was treated intraperitoneally (i.p.) with saline; positive control group was administered GM 60 mg/kg/day i.p.; RM group was co-administered 8% RM aqueous extract, 10 mL/kg/day, orally with GM; and TV group was co-administered 8% TV aqueous extract orally, 10 mL/kg/day with GM. Both RM and TV groups extracted significantly ameliorated plasma kidney function biomarkers, and reduced malondialdhyde and glucose levels. Meanwhile, RM extract significantly modulated the electrolyte concentration and increased plasma insulin levels as compared with the GM group. However, the aqueous extract of RM showed more pronounced effects than TV extract. Our data were confirmed by histopathological examination and deoxyribonucleic acid (DNA) fragmentation analysis. Deleterious histopathological changes and increased DNA fragmentation induced by GM treatment were markedly controlled by the co-administration of RM and TV. Such renoprotective influence of RM and TV suggests their concurrent supplementation with GM therapy to limit GM toxicity.


Subject(s)
Anti-Bacterial Agents/toxicity , Gentamicins/toxicity , Kidney/drug effects , Phytotherapy/methods , Plant Extracts/pharmacology , Protective Agents/pharmacology , Rosmarinus , Thymus Plant , Animals , Blood Glucose/drug effects , Drug Therapy, Combination , Insulin/blood , Kidney/metabolism , Kidney/pathology , Kidney Function Tests , Male , Malondialdehyde/metabolism , Plant Extracts/administration & dosage , Protective Agents/administration & dosage , Rats , Rats, Sprague-Dawley
6.
J Diet Suppl ; 10(3): 195-209, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23927622

ABSTRACT

Ginger is a remedy known to possess a number of pharmacological properties. This study investigated efficacy of ginger pretreatment in alleviating acetaminophen-induced acute hepatotoxicity in rats. Rats were divided into six groups; negative control, acetaminophen (APAP) (600 mg/kg single intraperitoneal injection); vitamin E (75 mg/kg), ginger (100 mg/kg), vitamin E + APAP, and ginger + APAP. Administration of APAP elicited significant liver injury that was manifested by remarkable increase in plasma alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), arginase activities, and total bilirubin concentration. Meanwhile, APAP significantly decreased plasma total proteins and albumin levels. APAP administration resulted in substantial increase in each of plasma triacylglycerols (TAGs), malondialdhyde (MDA) levels, and total antioxidant capacity (TAC). However, ginger or vitamin E treatment prior to APAP showed significant hepatoprotective effect by lowering the hepatic marker enzymes (AST, ALT, ALP, and arginase) and total bilirubin in plasma. In addition, they remarkably ameliorated the APAP-induced oxidative stress by inhibiting lipid peroxidation (MDA). Pretreatment by ginger or vitamin E significantly restored TAGs, and total protein levels. Histopathological examination of APAP treated rats showed alterations in normal hepatic histoarchitecture, with necrosis and vacuolization of cells. These alterations were substantially decreased by ginger or vitamin E. Our results demonstrated that ginger can prevent hepatic injuries, alleviating oxidative stress in a manner comparable to that of vitamin E. Combination therapy of ginger and APAP is recommended especially in cases with hepatic disorders or when high doses of APAP are required.


Subject(s)
Acetaminophen/adverse effects , Antioxidants/therapeutic use , Chemical and Drug Induced Liver Injury/drug therapy , Liver/drug effects , Phytotherapy , Vitamin E/therapeutic use , Zingiber officinale , Alanine Transaminase/blood , Analgesics, Non-Narcotic/adverse effects , Animals , Antioxidants/pharmacology , Aspartate Aminotransferases/blood , Bilirubin/blood , Blood Proteins/metabolism , Chemical and Drug Induced Liver Injury/blood , Chemical and Drug Induced Liver Injury/pathology , Lipid Peroxidation/drug effects , Liver/enzymology , Male , Malondialdehyde/blood , Necrosis , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Rats , Rats, Sprague-Dawley , Triglycerides/blood , Vitamin E/pharmacology
7.
Toxicol Ind Health ; 29(4): 367-84, 2013 May.
Article in English | MEDLINE | ID: mdl-22301819

ABSTRACT

Developmental disorders (DDs) are important leading cause of disability in developed countries and also in the United States. DDs are a group of individual conditions that result from abnormal nervous system development and cause altered function. They can begin at any time from prenatal to 22 years of age and the disability usually presents itself throughout a person's life time. Down syndrome, autism, neural tube defects, schizophrenia, cretinism, and attention-deficit hyperactivity disorder are among the most common DDs that currently plague numerous countries and have varying incidence rates. Their occurrence may be partially attributable to the lack of certain dietary nutrients. Notably, essential vitamins, minerals, and ω-3 fatty acids are often deficient in the general population of America and developed countries and are exceptionally deficient in patients suffering from mental disorders. Typically, most of these disorders are treated with prescription drugs, but many of these drugs cause unwanted side effects. Therefore, psychiatrists recommend alternative or complementary nutritional remedies to overcome the adverse effects of those drugs. Studies have shown that daily supplements of vital nutrients, such as that contain amino acids, often effectively reduce symptoms of the patients, because they are converted into neurotransmitters that alleviate depression and other mental disorders. The aim of this article is to discuss the role of dietary imbalances in the incidence of DD and to emphasize which dietary supplements can aid in the treatment of the above-mentioned DD.


Subject(s)
Developmental Disabilities/diet therapy , Developmental Disabilities/etiology , Diet , Dietary Supplements , Learning Disabilities/diet therapy , Plant Extracts/administration & dosage , Antioxidants/administration & dosage , Humans
8.
Indian J Exp Biol ; 40(1): 45-8, 2002 Jan.
Article in English | MEDLINE | ID: mdl-12561967

ABSTRACT

A significant increase in body weight with remarkable increase in total food intake and significant increase in protein efficiency ratio were observed following oral administration of R. graveolens ether extract (500 mg/kg body wt) to growing rats for 3 weeks. Serum albumin was significantly decreased after administration of declofenac (15 mg/kg body wt). Albumin/globulin ratio decreased significantly on administration of E. peplus ether extract (500 mg/kg body wt). No significant changes were observed in other biochemical and nutritional parameters on administration of either of the extracts or declofenac. However, only a significant elevation of alkaline phosphatase was noticed during treatment with R. graveolens. The results suggest that both plant extracts have no harmful effect on nutritional status and are safe towards kidney functions, while Euphorbia is more safe than Ruta in relation to liver functions.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Euphorbia/chemistry , Nutritional Status/drug effects , Plant Extracts/pharmacology , Plants, Medicinal , Ruta/chemistry , Administration, Oral , Alkaline Phosphatase/metabolism , Animals , Anti-Inflammatory Agents/administration & dosage , Body Weight/drug effects , Energy Intake , Phytotherapy , Plant Extracts/administration & dosage , Rats , Rats, Inbred Strains , Safety , Serum Albumin/analysis
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